HCID 86658574, Verbindung → HCID 67433397, Verbindung
Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:23]=[CH:22][C:6]([CH2:7][N:8]2[C:12](/[CH:13]=[CH:14]/[O:15][CH3:16])=[C:11]([C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH:10]=[N:9]2)=[CH:5][CH:4]=1>CO.[Pd]>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][N:8]2[C:12]([CH2:13][CH2:14][O:15][CH3:16])=[C:11]([C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH:10]=[N:9]2)=[CH:22][CH:23]=1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
According to Scheme 17 Step 3: To a mixture of (E)-ethyl 1-(4-methoxybenzyl)-5-(2-methoxyvinyl)-1H-pyrazole-4-carboxylate (1.58 mmol, 500 mg) in MeOH (7.9 mL) was hydrogenated in a H-Cube® with Pd/C under a 20 bar H2 atmosphere. The reaction mixture was filtered through celite and the filtrate was concentrated to dryness to afford ethyl 1-(4-methoxybenzyl)-5-(2-methoxyethyl)-1H-pyrazole-4-carboxylate (1.57 mmol, 500 mg, 99%).
Aufarbeitung
- filtrationThe reaction mixture was filtered through celite
- concentrationthe filtrate was concentrated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-6dbec415e39f47328f1f34c43357d09d
- Quelldatensatz
- uspto-grants-2015_07
- Patentnummer
- US09073907B2
Notizen zur Reaktion
Wird geladen…